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CAS 160982-11-6

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3-(2-Bromoacetyl)-5-chloro-2-thiophenesulfonamide

Description:
3-(2-Bromoacetyl)-5-chloro-2-thiophenesulfonamide is a chemical compound characterized by its unique structure, which includes a thiophene ring, a sulfonamide group, and halogen substituents. The presence of the bromoacetyl group introduces a reactive site that can participate in various chemical reactions, making it useful in synthetic organic chemistry. The chloro substituent enhances the compound's reactivity and may influence its biological activity. This compound is typically solid at room temperature and may exhibit moderate solubility in polar solvents due to the sulfonamide functional group. Its sulfonamide moiety suggests potential applications in medicinal chemistry, particularly in the development of antimicrobial agents. Additionally, the presence of halogens can affect the compound's electronic properties, potentially impacting its interaction with biological targets. As with many synthetic compounds, safety precautions should be observed when handling, as it may pose health risks or environmental hazards. Overall, this compound's distinctive features make it a subject of interest in both research and industrial applications.
Formula:C6H5BrClNO3S2
InChI:InChI=1S/C6H5BrClNO3S2/c7-2-4(10)3-1-5(8)13-6(3)14(9,11)12/h1H,2H2,(H2,9,11,12)
InChI key:InChIKey=OZESFFKYLOCAOV-UHFFFAOYSA-N
SMILES:S(N)(=O)(=O)C1=C(C(CBr)=O)C=C(Cl)S1
Synonyms:
  • 2-Thiophenesulfonamide, 3-(2-bromoacetyl)-5-chloro-
  • 2-Thiophenesulfonamide, 3-(bromoacetyl)-5-chloro-
  • 3-(2-Bromoacetyl)-5-chloro-2-thiophenesulfonamide
  • 3-(Bromoacetyl)-5-Chlorothiophene-2-Sulfonamide
  • 3-(Bromoacetyl)-5-chloro-2-thiophenesulfonamide
  • 3-Bromoacetyl-5-Chloro-2-Thiophenesulfonamide
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